G. Fontaine et al., THE DURATION OF QRS COMPLEXES IN ARRHYTHM OGENIC RIGHT-VENTRICULAR DYSPLASIA - A NEW NONINVASIVE DIAGNOSTIC-TOOL, Annales de cardiologie et d'angeiologie, 42(8), 1993, pp. 399-405
Arrhythmogenic right ventricular dysplasia (ARVD) may result in sudden
death of young and sometimes athletic individuals, while if properly
treated it is associated with a good prognosis. It is probably more wi
despread than currently thought. Comparison of the electrocardiograms
of 43 ARVD patients with those of 44 normal individuals provided a new
criterion enabling identification of the disease. Measurement of a QR
S interval longer than 110 ms in sinus rhythm in lead V1 in an individ
ual with an apparently normal heart enabled identification of the dise
ase with a sensitivity of 55 p. cent and specificity of 100 p. cent if
used alone, and a sensitivity of 60 p. cent if used in combination wi
th a prolongation of QRS in lead V3 to greater than 110 ms, but with a
specificity of 82 p. cent. After elimination of appearances of right
bundle branch block, sensitivity was 50 p. cent for V1, This parameter
studied in a hospital population should be validated in minor forms b
efore leading to compulsory ECGs for individuals in high-risk occupati
ons (athletes, public vehicle drivers, etc.).